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EC number: 288-752-8 | CAS number: 85895-78-9
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- activated sludge respiration inhibition testing
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 2006-11-06 to 2007-02-27
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Justification for type of information:
- For details and justification of read-across please refer to the read-across report attached to IUCLID section 13.
- Reason / purpose for cross-reference:
- read-across source
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 209 (Activated Sludge, Respiration Inhibition Test
- Version / remarks:
- April 4, 1984
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- Municipal sewage treatment plant: 'Waterschap de Maaskant', 's-Hertogenbosch, the Netherlands, receiving predominantly domestic sewage.
The sludge was coarsely sieved, washed and diluted with ISO-medium. A small amount of the sludge was weighed and dried overnight at ca. 105 °C to determine the amount of suspended solids (4.3 g/L of sludge, as used for the test). The pH was 7.8 on the day of sampling and 7.5 on the day of testing. The batch of sludge was used one day after collection; therefore 50 mL of synthetic sewage feed was added per litre of activated sludge at the end of the collection day. The sludge was kept aerated at test temperature until use. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- yes
- Total exposure duration:
- 3 h
- Test temperature:
- 18–18.6 °C
- pH:
- 7.9
- Dissolved oxygen:
- 7.7–7.8 mg/L
- Nominal and measured concentrations:
- 100 mg/L test material nominal (88 mg/L active substance nominal).
- Details on test conditions:
- Type: other: Activated sludge respiration inhibition test
TEST SYSTEM
- Test vessel: All glass, approximately 300 mL oxygen bottles and 1 litre test bottles.
TEST MEDIUM/WATER PARAMETERS
Adjusted ISO medium, formulated using RO-water (tap-water purified by reverse osmosis; GEON Waterbehandeling, Berkel-Enschot, The Netherlands) with the following composition:
CaCI2.2H2O 211.5 mg/L
MgSO4.7H2O 88.8 mg/L
NaHCO3 46.7 mg/L
KCl 4.2 mg/L
SYNTHETIC SEWAGE FEED
16 g peptone 11 g meat extract
3 g urea
0.7 g NaCI
0.4 g CaCI2.2H2O
0.2 g MgSO4.7H2O
2.8 g K2HPO4
Dissolved in Milli-Q water, made up to 1 litre and filtered.
The pH was adjusted from 6.8 to 7.0 with 1 M NaOH (Merck, Darmstadt, Germany).
EFFECT PARAMETERS MEASURED (with observation intervals if applicable):
Oxygen consumption
TEST CONCENTRATIONS
Limit test - Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichlorophenol
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 100 mg/L
- Results with reference substance (positive control):
- - Results with reference substance valid? Yes
- Relevant effect levels: EC50 5.9 mg/L - Validity criteria fulfilled:
- yes
- Conclusions:
- Lactic acid 88.3 % does not inhibit activated sludge respiration at concentrations up to 100 mg/L test material (88.3 mg/L active substance). Inhibition was -1.1% (stimulation).
- Executive summary:
The influence of PURAC HS 88 on the respiration rate of activated sludge was investigated after a contact time of 3 hours. The study procedure was based on OECD guideline no. 209, adopted April 4, 1984, EEC Directive 67/548, amended November 18, 1987 (87/302), part C, publication no. L133, adopted May 30, 1988, and ISO standard 8192 (1986).
The batch of PURAC HS 88 was a clear and colourless liquid that easily dissolved in water. A stock solution of 500 mg/L was prepared by adding 126.0 mg test substance to 250 mL of Milli- RO water. A stirring period of 30 minutes was used to accelerate dissolution and to ensure homogeneity. Volumes of the stock solution corresponding to the test concentration were then added to the test media. A concentration of 100 mg/L was tested in duplicate. Optimal contact between the test substance and test medium was ensured applying continuous aeration and stirring.
No significant inhibition of respiration rate of the sludge was recorded at 100 mg PURAC HS 88 per litre. The duplicate measurement confirmed the result of the first measurement. Therefore no further testing was needed.
Since all criteria for acceptability of the test were met, this study was considered to be valid.
In conclusion, under the conditions of this present test, PURAC HS 88 was not toxic to waste water (activated sludge) bacteria at a concentration of 100 mg/L.
This information is used in a read-across approach in the assessment of the target substance. For details and justification of read-across please refer to the read-across report attached to IUCLID section 13.
Reference
Description of key information
L(+) lactic acid is not toxic to wastewater (activated sludge) bacteria at a concentration of 100 mg/L (equalling 88 mg lactate/L). Potassium is not expected to make any contribution to potential toxicity to microorganisms. Therefore, no hazard of potassium-S-lactate to microorganisms is identified.
Key value for chemical safety assessment
- EC10 or NOEC for microorganisms:
- 100 mg/L
Additional information
This information is used in a read-across approach in the assessment of the target substance. For details and justification of read-across please refer to the read-across report attached to IUCLID section 13.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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